The human H-twist gene is located at 7p21 and encodes a B-HLH protein that is 96% similar to its murine M-twist counterpart.

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作者信息

Bourgeois P, Stoetzel C, Bolcato-Bellemin A L, Mattei M G, Perrin-Schmitt F

机构信息

Institut de Chimie Biologique--Faculté de Médecine, LGME du CNRS--U 184 de l'INSERM, Strasbourg, France.

出版信息

Mamm Genome. 1996 Dec;7(12):915-7. doi: 10.1007/s003359900269.

DOI:10.1007/s003359900269

PMID:8995765

Abstract

摘要

相似文献

The human H-twist gene is located at 7p21 and encodes a B-HLH protein that is 96% similar to its murine M-twist counterpart.

Mamm Genome. 1996 Dec;7(12):915-7. doi: 10.1007/s003359900269.

Mutations of the TWIST gene in the Saethre-Chotzen syndrome.塞-乔二氏综合征中TWIST基因的突变。

Nat Genet. 1997 Jan;15(1):42-6. doi: 10.1038/ng0197-42.

The locations of the H-twist and H-dermo-1 genes are distinct on the human genome.H-twist和H-dermo-1基因在人类基因组上的位置不同。

Biochim Biophys Acta. 1997 Feb 27;1360(1):1-2. doi: 10.1016/s0925-4439(96)00071-3.

N-twist, an evolutionarily conserved bHLH protein expressed in the developing CNS, functions as a transcriptional inhibitor.N-twist是一种在发育中的中枢神经系统中表达的进化保守的bHLH蛋白，作为转录抑制剂发挥作用。

Dev Biol. 2002 Sep 1;249(1):174-90. doi: 10.1006/dbio.2002.0753.

Twist and shout.扭动并呼喊。

Nat Genet. 1997 Jan;15(1):3-4. doi: 10.1038/ng0197-3.

A leech homolog of twist: evidence for its inheritance as a maternal mRNA.一种与twist同源的水蛭蛋白：作为母体mRNA遗传的证据。

Gene. 1997 Oct 15;199(1-2):31-7. doi: 10.1016/s0378-1119(97)00327-2.

Human Dermo-1 has attributes similar to twist in early bone development.人类真皮-1在早期骨骼发育中具有与 Twist 相似的特性。

Bone. 2000 Nov;27(5):591-602. doi: 10.1016/s8756-3282(00)00380-x.

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome.塞特勒-乔岑综合征中，一种基本的螺旋-环-螺旋转录因子TWIST的突变。

Nat Genet. 1997 Jan;15(1):36-41. doi: 10.1038/ng0197-36.

A myogenic switch. Muscle development.

Curr Biol. 1996 Aug 1;6(8):924-6. doi: 10.1016/s0960-9822(02)00627-9.

A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1.对颅缝早闭患者进行TWIST突变的全面筛查，发现了一种新的7号染色体7p21.1带微缺失综合征。

Am J Hum Genet. 1998 Nov;63(5):1282-93. doi: 10.1086/302122.

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Twist alters the breast tumor microenvironment via choline kinase to facilitate an aggressive phenotype.Twist 通过胆碱激酶改变乳腺肿瘤微环境，促进侵袭表型。

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The speckle-type POZ protein (SPOP) inhibits breast cancer malignancy by destabilizing TWIST1.斑点型POZ蛋白（SPOP）通过使TWIST1不稳定来抑制乳腺癌的恶性程度。

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Downregulation of hsa_circ_0001681 suppresses epithelial-mesenchymal transition in thyroid carcinoma via targeting to miR-942-5p/TWIST1 signaling pathway.hsa_circ_0001681 的下调通过靶向 miR-942-5p/TWIST1 信号通路抑制甲状腺癌中的上皮-间充质转化。

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MYB Proto-oncogene-like 1-TWIST1 Axis Promotes Growth and Metastasis of Hepatocellular Carcinoma Cells.MYB原癌基因样1-TWIST1轴促进肝癌细胞的生长和转移。

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The Changes of Twist1 Pathway in Pulmonary Microvascular Permeability in a Newborn Rat Model of Hyperoxia-Induced Acute Lung Injury.高氧诱导新生大鼠急性肺损伤模型中Twist1通路在肺微血管通透性中的变化

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Vasculogenic mimicry and expression of Twist1 and KAI1 correlate with metastasis and prognosis in lung squamous cell carcinoma.血管生成拟态以及Twist1和KAI1的表达与肺鳞状细胞癌的转移和预后相关。

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本文引用的文献

Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching.通过EST数据库搜索鉴定与果蝇突变基因同源的人类cDNA并进行图谱绘制。

Nat Genet. 1996 Jun;13(2):167-74. doi: 10.1038/ng0696-167.

The B-HLH protein encoding the M-twist gene is located by in situ hybridization on murine chromosome 12.编码M-twist基因的B-HLH蛋白通过原位杂交定位在小鼠12号染色体上。

Mamm Genome. 1993;4(2):127-8. doi: 10.1007/BF00290439.

Loci for autosomal dominant retinitis pigmentosa and dominant cystoid macular dystrophy on chromosome 7p are not allelic.位于7号染色体短臂上的常染色体显性遗传性视网膜色素变性和显性黄斑囊样变性的基因座并非等位基因。

Am J Hum Genet. 1994 Sep;55(3):581-2.

Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p.

Hum Mol Genet. 1994 Feb;3(2):299-302. doi: 10.1093/hmg/3.2.299.

Localization of the genetic locus for Saethre-Chotzen syndrome to a 6 cM region of chromosome 7 using four cases with apparently balanced translocations at 7p21.2.

Hum Mol Genet. 1994 Aug;3(8):1405-8. doi: 10.1093/hmg/3.8.1405.

Dorso-ventral and rostro-caudal sequential expression of M-twist in the postimplantation murine embryo.植入后小鼠胚胎中M-twist的背腹向和头尾向顺序表达。

Mech Dev. 1995 Jun;51(2-3):251-63. doi: 10.1016/0925-4773(95)00369-x.

Determination of nucleotide sequences in DNA.DNA中核苷酸序列的测定。

Science. 1981 Dec 11;214(4526):1205-10. doi: 10.1126/science.7302589.

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome.通过原位杂交将DNA探针定位在18p11.3带，并鉴定出一条小的额外染色体。

Hum Genet. 1985;69(3):268-71. doi: 10.1007/BF00293038.

De novo del(7)(pter----p21.2::p15.2----qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndrome.

Ann Genet. 1986;29(1):36-8.

Sequence of the twist gene and nuclear localization of its protein in endomesodermal cells of early Drosophila embryos.果蝇早期胚胎内胚层中twist基因序列及其蛋白质的核定位

EMBO J. 1988 Jul;7(7):2175-83. doi: 10.1002/j.1460-2075.1988.tb03056.x.

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